The triple screening procedures the amount of three substances in a pregnant woman’s blood:

  • Alpha-fetoprotein (AFP)
  • Human chorionic Gonadotropin (HCG) and
  • Estriol (uE3)

When a test for the hormone inhibin A is added, then these tests are called the maternal serum triple test, the expanded AFP test, the AFP plus test, or the multiple marker screening tests.

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The amounts of these substances help your doctor find out the chance that your baby has certain birth defects, such as Down syndrome, spina bifida or anencephaly. You would need a diagnostic test called amniocentesis to find out for sure if there is a problem. The triple screening is usually done at 15 to 20 weeks of pregnancy.

Each substance tested in a triple screening gives you different information about possible problems. Together, these results give the best information. These screening tests look for the amount of:

  • Alpha-fetoprotein (AFP) Alpha-fetoprotein (AFP), which is made by the baby’s liver.
  • Human chorionic gonadotrophin (HCG) Human chorionic gonadotrophin (HCG), a hormone made by the placenta when a woman becomes pregnant.
  • Estriol (uE3), a form of estrogen that increases during pregnancy. It is produced in large amounts by the placenta.
  • Hormone inhibin A, a protein produced by the baby and the placenta.

A simple blood test is all that’s needed for these tests. The health specialist taking a sample of your blood will:

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  • Wrap an elastic band around your upper arm. This makes the veins below the band larger so it is easier to put a needle into the vein.
  • Clean the needle site with alcohol.
  • Put the needle into the vein.
  • Attach a tube to the needle to fill it with blood.
  • Remove the band from your arm when enough blood is collected.
  • Put a gauze pad or cotton ball over the needle site as the needle is removed.
  • Put pressure on the site and then put on a bandage.

This tests helps parents prepare for birth. If all the results are ordinary, parents know that they are less expected to have a baby with a genetic disorder.